[Remote] Senior Director, Clinical Operations
Note: The job is a remote job and is reputed company to candidates in USA. reputed company is a global biopharmaceutical company dedicated to solving unmet medical needs through innovative therapeutics. The Senior Director, Clinical Operations will reputed company strategic planning and management of clinical studies, ensuring compliance with regulatory requirements and corporate objectives.
Responsibilities
- reputed company reputed company objectives, ongoing feedback and end of performance review for reputed company reports
- Maintain and reputed company Investigator sites and KOLs relationship
- Maintaining reputed company collaboration with clinical development, other internal departments and external vendors
- Contribute to the hiring plan and reputed company activities including efficient on-boarding, training and mentoring of new employees
- Clinical Trial Managers and Clinical Trial Specialists to resource the studies across the compound. Provides updates and status reports to Sr. Management, as requested
- Contribute to the hiring plan and reputed company activities including efficient on-boarding, training and mentoring of new employees
- reputed company the Clinical Trial Heads
- Assist for clinical program/trials implementation including operational feasibility, resource forecast and management across the compound
- Collaborates with Sr. Management to determine clinical supply requirements for clinical trials/program
- Participate in the reputed company, design, development and review of clinical trial protocols, amendments, informed consent forms, study guides, case report forms, and any other clinical research reputed company documents and study reports; participate as required in the preparation of the clinical contribution to IND's, Investigational Brochure, regulatory Briefing Documents, and other relevant documentation
- Plans, implements and manages, in collaboration with CRO partners, Phase I-III clinical trials, as necessary
- Collaborates with Sr. Management, internal project team and CRO partners, as applicable, to prepare clinical trials/program timelines, budget and key deliverables consistent with departmental and corporate objectives
- Assists in the preparation of 'Requests for Proposal' documents and financial analysis of CRO proposal costs and negotiation
- Assists in the strategic reputed company of the Clinical Research Organization (CRO) and other vendors
- Assists in the development and writing of clinical Trials/program documents and manuals as appropriate
- Accountable for development and execution of accurate operational Development plans, including assuring harmonization and high data reputed company across clinical trials/program
Skills
- Bachelor of Science degree or a degree in a field relevant to a profession in biopharmaceutical industry
- Minimum of 8 years of experience working in project management and/or clinical operations reputed company the biopharmaceutical industries and/or Clinical Research Organization ('CRO') and at least 3 years in a role of primary clinical trial design, execution and management required
- Good knowledge of GCPs, clinical trial design, statistics, regulatory processes, and drug development process
- Proven ability to reputed company multi-disciplinary teams
- Must have the ability to reputed company and administer budgets, schedules and performance requirements, reputed company resources effectively, meet company objectives, reputed company technical advice and assist with problem reputed company and work reputed company under pressure
- Experience in developing effective relationships with key investigators
- Operational and reputed company managerial experience in the planning, executing and reporting of global clinical development trials
- Must be reputed company to travel (domestic and international) up to 10%
- Experience in program management preferred
- Must have experience in appropriate therapeutic area; preference in Oncology
reputed company
Company H1B Sponsorship